Brugada syndrome genetics is associated with phenotype severity

AIMS : Brugada syndrome (BrS) is associated with an increased risk of sudden cardiac death due to ventricular tachycardia/fibrillation (VT/VF) in young, otherwise healthy individuals. Despite SCN5A being the most commonly known mutated gene to date, the genotype–phenotype relationship is poorly unde...

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Detaylı Bibliyografya
Yayımlandı:Eur Heart J
Asıl Yazarlar: Ciconte, Giuseppe, Monasky, Michelle M, Santinelli, Vincenzo, Micaglio, Emanuele, Vicedomini, Gabriele, Anastasia, Luigi, Negro, Gabriele, Borrelli, Valeria, Giannelli, Luigi, Santini, Francesca, de Innocentiis, Carlo, Rondine, Roberto, Locati, Emanuela T, Bernardini, Andrea, Mazza, Beniamino C, Mecarocci, Valerio, Ćalović, Žarko, Ghiroldi, Andrea, D’Imperio, Sara, Benedetti, Sara, Di Resta, Chiara, Rivolta, Ilaria, Casari, Giorgio, Petretto, Enrico, Pappone, Carlo
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Oxford University Press 2020
Konular:
Clnical Research
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC7955973/
https://ncbi.nlm.nih.gov/pubmed/33221895
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/eurheartj/ehaa942
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